Evidence map›Paper›PMID 20948988›Full record

ArticleApplied soft computing2007

Genetic Programming Neural Networks: A Powerful Bioinformatics Tool for Human Genetics.

Marylyn D Ritchie, Alison A Motsinger, William S Bush, Christopher S Coffey, Jason H Moore

Abstract read
In one paragraph

Article in Applied soft computing, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
  2. Gene-gene interaction: the curse of dimensionality.Annals of translational medicine · 2019
    Review
  3. Robust genetic interaction analysis.Briefings in bioinformatics · 2019
    Review
  4. Article
  5. Statistical and Computational Methods for Genetic Diseases: An Overview.Computational and mathematical methods in medicine · 2015
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. A Bayesian method for identifying genetic interactions.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2009
    Article
  14. Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Marylyn D RitchieCenter for Human Genetics Research, Department of Molecular Physiology and Biophysics, Vanderbilt University, 519 Light Hall, Nashville, TN 37232.
Alison A Motsinger
William S Bush
Christopher S Coffey
Jason H Moore

Funding

PHARMACOGENOMICS OF ARRHYTHMIA THERAPYU01HL065962 · NHLBI · VANDERBILT UNIVERSITY · PI RODEN, DAN M · 2001 to 2009
$24.8M
Vanderbilt Biomedical Informatics Training ProgramT15LM007450 · NLM · VANDERBILT UNIVERSITY · PI Jessica S. Ancker, Bradley A. Malin · 2002 to 2026
$19.7M
Pharmacogenomics of Arrhythmia TherapyU19HL065962 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RODEN, DAN M · 2010 to 2014
$17.4M
Genetic Studies of Dementia in the AmishR01AG019085 · NIA · VANDERBILT UNIVERSITY · PI HAINES, JONATHAN L · 2001 to 2011
$11.0M
YOHIMBINE THERAPY IN AUTONOMIC FAILUREP01GM031304 · NIGMS · VANDERBILT UNIVERSITY · PI STEIN, CHARLES M. · 1985 to 2006
$8.1M
Bioinformatics Strategies: Biodefense Vaccine ResearchR01AI059694 · NIAID · DARTMOUTH COLLEGE · PI MOORE, JASON H. · 2004 to 2012
$4.5M
Revealing Epistasis in Alzheimer DiseaseR01AG020135 · NIA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MARTIN, EDEN R. · 2002 to 2006
$2.7M
Genetics Basis of Trauma RecoveryR01HD047447 · NICHD · DARTMOUTH COLLEGE · PI MOORE, JASON H. · 2005 to 2009
$1.8M
GENETIC ARCHITECTURE OF PLASMA T-PA AND PAI-1R01HL065234 · NHLBI · VANDERBILT UNIVERSITY · PI MOORE, JASON H. · 2000 to 2004
$1.7M
NHLBI NIH HHS R01 HL065234NHLBI NIH HHS U01 HL065962NHLBI NIH HHS U19 HL065962NIAID NIH HHS R01 AI059694NIA NIH HHS R01 AG019085NIA NIH HHS R01 AG020135NICHD NIH HHS R01 HD047447NIGMS NIH HHS P01 GM031304NLM NIH HHS T15 LM007450
6 · The paper itself

Abstract

The identification of genes that influence the risk of common, complex disease primarily through interactions with other genes and environmental factors remains a statistical and computational challenge in genetic epidemiology. This challenge is partly due to the limitations of parametric statistical methods for detecting genetic effects that are dependent solely or partially on interactions. We have previously introduced a genetic programming neural network (GPNN) as a method for optimizing the architecture of a neural network to improve the identification of genetic and gene-environment combinations associated with disease risk. Previous empirical studies suggest GPNN has excellent power for identifying gene-gene and gene-environment interactions. The goal of this study was to compare the power of GPNN to stepwise logistic regression (SLR) and classification and regression trees (CART) for identifying gene-gene and gene-environment interactions. SLR and CART are standard methods of analysis for genetic association studies. Using simulated data, we show that GPNN has higher power to identify gene-gene and gene-environment interactions than SLR and CART. These results indicate that GPNN may be a useful pattern recognition approach for detecting gene-gene and gene-environment interactions in studies of human disease.

Identifiers

PMID20948988
PMCPMC2952963

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.